Vertebrate Endoderm Development and Organ Formation

Wnt/β-Catenin Signaling in Development and Disease

Clevers, H. (2006) · Cell · doi:10.1016/j.cell.2006.10.018 · Cited by 5,568

Production of pancreatic hormone–expressing endocrine cells from human embryonic stem cells

D’Amour, K. A., Bang, A. G., Eliazer, S., Kelly, O., Agulnick, A. D., Smart, N. G., Moorman, M. A., KROON, E. J., Carpenter, M. K., & Baetge, E. E. (2006) · Nature Biotechnology · doi:10.1038/nbt1259 · Cited by 1,913

Pancreatic endoderm derived from human embryonic stem cells generates glucose-responsive insulin-secreting cells in vivo

Kroon, E., Martinson, L. A., Kadoya, K., Bang, A. G., Kelly, O. G., Eliazer, S., Young, H., Richardson, M., Smart, N. G., Cunningham, J., et al. (2008) · Nature Biotechnology · doi:10.1038/nbt1393 · Cited by 1,843

Efficient differentiation of human embryonic stem cells to definitive endoderm

D'Amour, K. A., Agulnick, A. D., Eliazer, S., Kelly, O. G., Kroon, E., & Baetge, E. E. (2005) · Nature Biotechnology · doi:10.1038/nbt1163 · Cited by 1,730

Retinoic Acid Synthesis and Signaling during Early Organogenesis

Duester, G. (2008) · Cell · doi:10.1016/j.cell.2008.09.002 · Cited by 1,098

Development of definitive endoderm from embryonic stem cells in culture

Kubo, A., Shinozaki, K., Shannon, J. M., Kouskoff, V., Kennedy, M., Woo, S. L. C., Fehling, H. J., & Keller, G. M. (2004) · Development · doi:10.1242/dev.01044 · Cited by 830

Initiation of Mammalian Liver Development from Endoderm by Fibroblast Growth Factors

Jung, J., Zheng, M., Goldfarb, M., & Zaret, K. S. (1999) · Science · doi:10.1126/science.284.5422.1998 · Cited by 721

Depletion of definitive gut endoderm in Sox17 -null mutant mice

Kanai-Azuma, M., Kanai, Y., Gad, J. M., Tajima, Y., Taya, C., Kurohmaru, M., Sanai, Y., Yonekawa, H., Yazaki, K., Tam, P. P. L., et al. (2002) · Development · doi:10.1242/dev.129.10.2367 · Cited by 704

Origin and organization of the zebrafish fate map

Kimmel, C. B., Warga, R. M., & Schilling, T. F. (1990) · Development · doi:10.1242/dev.108.4.581 · Cited by 698

FGF Signaling Regulates Mesoderm Cell Fate Specification and Morphogenetic Movement at the Primitive Streak

Ciruna, B. G., & Rossant, J. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00017-x · Cited by 695

Mitogen Synergy: An Emerging Route to Boosting Human Beta Cell Proliferation

Shcheglova, E. G., Błaszczyk, K., & Borowiak, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.734597 · Cited by 18

Generation of esophageal organoids and organotypic raft cultures from human pluripotent stem cells

Shacham-Silverberg, V., & Wells, J. M. (2020) · Methods in cell biology · doi:10.1016/bs.mcb.2020.04.009 · Cited by 16

Wnt signaling promotes hindgut fate commitment through regulating multi-lineage genes during hESC differentiation

Zhang, X., Chen, Y., Ye, Y., Wang, J., Wang, H., Yuan, G., Lin, Z., Wu, Y., Zhang, Y., & Lin, X. (2016) · Cellular Signalling · doi:10.1016/j.cellsig.2016.09.009 · Cited by 16

Production of high purity alveolar-like cells from iPSCs through depletion of uncommitted cells after AFE induction

Mitchell, A., Drinnan, C. T., Jensen, T., & Finck, C. M. (2017) · Differentiation · doi:10.1016/j.diff.2017.08.001 · Cited by 16

Development of the Taste System

Krimm, R. F., Thirumangalathu, S., & Barlow, L. A. (2015) · Wiley eBooks · doi:10.1002/9781118971758.ch33 · Cited by 16

Improved Tol2-mediated enhancer trap identifies weakly expressed genes during liver and β cell development and regeneration in zebrafish

Zhong, Y., Huang, W., Du, J., Wang, Z., He, J., & Luo, L. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005568 · Cited by 15

Mechanically enhanced biogenesis of gut spheroids with instability-driven morphomechanics

Lin, F., Li, X., Sun, S., Li, Z., Lv, C.-L., Bai, J., Song, L., Han, Y., Li, B., Fu, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41760-2 · Cited by 15

A multimodal cross-species comparison of pancreas development

Yang, K., Spitzer, H., Sterr, M., Hrovatin, K., Sean de la, O., Zhang, X., Setyono, E. S. A., Ud‐Dean, M., Walzthoeni, T., Flisikowski, K., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64774-4 · Cited by 16

Three-dimensional reconstruction of the embryonic pancreas in the grass snake Natrix natrix L. (Lepidosauria, Serpentes) based on histological studies

Kowalska, M., Hermyt, M., & Rupik, W. (2016) · Zoology · doi:10.1016/j.zool.2016.11.001 · Cited by 15

Cell Expansion During Directed Differentiation of Stem Cells Toward the Hepatic Lineage

Raju, R., Chau, D., Cho, D. S., Park, Y., Verfaillie, C. M., & Hu, W. (2016) · Stem Cells and Development · doi:10.1089/scd.2016.0119 · Cited by 15

Rational design and optimization of synthetic gene switches for controlling cell-fate decisions in pluripotent stem cells

Haellman, V., Saxena, P., Jiang, Y., & Fussenegger, M. (2021) · Metabolic Engineering · doi:10.1016/j.ymben.2021.03.009 · Cited by 15

Perspectives of future lung toxicology studies using human pluripotent stem cells

Masui, A., Hirai, T., & Gotoh, S. (2022) · Archives of Toxicology · doi:10.1007/s00204-021-03188-9 · Cited by 16

Lung organoids: current strategies for generation and transplantation

Demchenko, A. G., Лавров, А. В., & Smirnikhina, S. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03686-x · Cited by 15

An In Vivo and In Vitro Evaluation of the Mutual Interactions between the Lung and the Large Intestine

Yin, L.-M., Zhang, G., Yan, X.-K., Wang, Y., Xu, Y., & Yang, Y. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/695641 · Cited by 15

Animal Models of Pancreas Development, Developmental Disorders, and Disease

Lorberbaum, D. S., Docherty, F. M., & Sussel, L. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-2389-2_3 · Cited by 18

Signaling reprogramming via Stat3 activation unravels high-fidelity human post-implantation embryo modeling

Chen, C., Wu, J., Wang, X., Chang, L., Wang, K., Wu, K., Guo, M., Li, H., Sun, F., Jiang, X., et al. (2025) · Cell stem cell · doi:10.1016/j.stem.2025.08.011 · Cited by 15

Dynamic network biomarker factors orchestrate cell-fate determination at tipping points during hESC differentiation

Li, L., Xu, Y., Yan, L., Li, X., Li, F., Liu, Z., Zhang, C., Lou, Y., Gao, D., Cheng, X., et al. (2022) · The Innovation · doi:10.1016/j.xinn.2022.100364 · Cited by 14

The road to regenerative liver therapies: the triumphs, trials and tribulations

Raju, R., Chau, D., Verfaillie, C. M., & Hu, W.-S. (2013) · Biotechnology Advances · doi:10.1016/j.biotechadv.2013.08.022 · Cited by 14

Effects of Precaudal Elongation on Visceral Topography in a Basal Clade of Ray‐Finned Fishes

Ward, A. B., & Kley, N. J. (2011) · The Anatomical Record · doi:10.1002/ar.21491 · Cited by 14

Minireview: Directed Differentiation and Encapsulation of Islet β-Cells—Recent Advances and Future Considerations

Tse, H. M., Kozlovskaya, V., Kharlampieva, E., & Hunter, C. S. (2015) · Molecular Endocrinology · doi:10.1210/me.2015-1085 · Cited by 15

FGF2 Inhibits Early Pancreatic Lineage Specification during Differentiation of Human Embryonic Stem Cells

Dettmer, R., Cirksena, K., Münchhoff, J., Kresse, J., Diekmann, U., Niwolik, I., Buettner, F. F. R., & Naujok, O. (2020) · Cells · doi:10.3390/cells9091927 · Cited by 16

Differentiation of Human Pluripotent Stem Cells Into Definitive Endoderm Cells in Various Flexible Three-Dimensional Cell Culture Systems: Possibilities and Limitations

Bogacheva, M. S., Harjumäki, R., Flander, E., Taalas, A., Bystriakova, M. A., Yliperttula, M. L., Xiang, X., Leung, A. W., & Lou, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.726499 · Cited by 14

Stem/progenitor cells in normal physiology and disease of the pancreas

Fallas, M. E. A., Pedraza‐Arévalo, S., Cujba, A.-M., Manea, T., Lambert, C., Morrugares, R., & Sancho, R. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111459 · Cited by 16

Loss of Pancreas upon Activated Wnt Signaling Is Concomitant with Emergence of Gastrointestinal Identity

Muñoz‐Bravo, J. L., Flores‐Martínez, Á., Herrero-Martín, G., Puri, S., Taketo, M. M., Rojas, A., Hebrok, M., & Cano, D. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164714 · Cited by 14

Beyond cancer genes: colorectal cancer as robust intrinsic states formed by molecular interactions

Yuan, R., Zhang, S., Yu, J., Huang, Y., Lu, D., Cheng, R., Huang, S., Ao, P., Zheng, S. S., Hood, L., et al. (2017) · Open Biology · doi:10.1098/rsob.170169 · Cited by 14

Tissue-Specific Localization NUCB2/nesfatin-1 in the Liver and Heart of Mouse Fetus

Sun, S., & Yang, H. (2018) · Development & Reproduction · doi:10.12717/dr.2018.22.4.331 · Cited by 14

Enhanced Maturity and Functionality of Vascular Human Liver Organoids through 3D Bioprinting and Pillar Plate Culture

Lekkala, V. K. R., Shrestha, S., Qaryoute, A. A., Dhinoja, S., Acharya, P., Raheem, A., Jagadeeswaran, P., & Lee, M. (2024) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.4c01658 · Cited by 13

Prenatal alcohol exposure and cellular differentiation: a role for Polycomb and Trithorax group proteins in FAS phenotypes?

Veazey, K. J. (2013) · Alcohol research · doi:10.35946/arcr.v35.1.09 · Cited by 13

Shared hemocyte- and intestine-dominant expression profiles of intelectin genes in ascidian Ciona intestinalis: insight into the evolution of the innate immune system in chordates

Hayashibe, M., Nakayama, S., & Ogasawara, M. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2647-3 · Cited by 13

Glypican 4 regulates planar cell polarity of endoderm cells by controlling the localization of Cadherin 2

Balaraju, A. K., Hu, B., Rodriguez, J. J., Murry, M., & Lin, F. H. (2021) · Development · doi:10.1242/dev.199421 · Cited by 13

Modeling Human Organ Development and Diseases With Fetal Tissue–Derived Organoids

Liang, J., Li, X., Dong, Y., & Zhao, B. T. (2022) · Cell Transplantation · doi:10.1177/09636897221124481 · Cited by 13

Short‐term and long‐term human or mouse organoid units generate tissue‐engineered small intestine without added signalling molecules

Hou, X., Chang, D. F., Trecartin, A., Barthel, E. R., Schlieve, C. R., Frey, M. R., Fowler, K. L., & Grikscheit, T. C. (2018) · Experimental Physiology · doi:10.1113/ep086990 · Cited by 13

Hepatic differentiation of mouse iPS cells and analysis of liver engraftment potential of multistage iPS progeny

Balasiddaiah, A., Moreno, D., Guembe, L., Prìeto, J., & Aldabe, R. (2013) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-013-0260-9 · Cited by 13

Human gastroids to model regional patterning in early stomach development

Li, X., Lin, F., Cui, Q., Sun, S., Li, S., Wang, Y., Wang, Y., Bai, J., Liu, S., Guo, J., et al. (2025) · Nature · doi:10.1038/s41586-025-09508-8 · Cited by 12

Generation of 3D lung organoids from human induced pluripotent stem cells for modeling of lung development and viral infection

Tiwari, S. K., & Rana, T. M. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e19601 · Cited by 12

Single-cell profiling of the pig cecum at various developmental stages

Xiao, Y., 江西农业大学猪遗传改良与种质创新全国重点实验室, 江. 南. 3., Zhang, Q., Huang, F., Rao, L., Yao, T., Yang, S., Xie, L., Zou, X.-X., Cai, L., et al. (2023) · 动物学研究 · doi:10.24272/j.issn.2095-8137.2023.007 · Cited by 13

Retinoic Acid and the Development of the Endoderm

Kelly, G. M., & Drysdale, T. A. (2015) · Journal of Developmental Biology · doi:10.3390/jdb3020025 · Cited by 12

Xenopus as a Model for GI/Pancreas Disease

Salanga, M. C., & Horb, M. E. (2015) · Current Pathobiology Reports · doi:10.1007/s40139-015-0076-0 · Cited by 12

Differentially expressed genes in Men1 knockout and wild‑type embryoid bodies for pancreatic islet development

Li (2011) · Molecular Medicine Reports · doi:10.3892/mmr.2011.409 · Cited by 12

The evolutionary acquisition and mode of functions of promoter-associated non-coding RNAs (pancRNAs) for mammalian development

An, B., Kameda, T., & Imamura, T. (2021) · Essays in Biochemistry · doi:10.1042/ebc20200143 · Cited by 12

Xenopus as a model system for studying pancreatic development and diabetes

Kofent, J., & Spagnoli, F. M. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.01.005 · Cited by 13

hPSC-derived lung organoids: Potential opportunities and challenges

Du, X., Dong, Y., Li, W., & Chen, Y. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e13498 · Cited by 11

A critical review on therapeutic approaches of CRISPR-Cas9 in diabetes mellitus

Bora, J., Dey, A., Lyngdoh, A. R., Dhasmana, A., Ranjan, A., Kishore, S., Rustagi, S., Tuli, H. S., Chauhan, A. P. S., Rath, P., et al. (2023) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-023-02631-1 · Cited by 14

Organogenetic transcriptomes of the Drosophila embryo at single cell resolution

Peng, D., Jackson, D. J., Palicha, B., Kernfeld, E. M., Laughner, N., Shoemaker, A. M., Celniker, S., Loganathan, R., Cahan, P., & Andrew, D. J. (2024) · Development · doi:10.1242/dev.202097 · Cited by 11

Histology Atlas of the Developing Mouse Respiratory System From Prenatal Day 9.0 Through Postnatal Day 30

Parslow, V., Elmore, S. A., Cochran, R. Z., Bolon, B. N., Mahler, B. W., Sabio, D. A., & Lubeck, B. A. (2024) · Toxicologic Pathology · doi:10.1177/01926233241252114 · Cited by 11

The kidney stroma in development and disease

Fusco, A. N., Oxburgh, L. H., & Carroll, T. J. (2025) · Nature Reviews Nephrology · doi:10.1038/s41581-025-00985-8 · Cited by 11

Molecular crosstalk in tracheal development and its recurrence in adult tissue regeneration

Kiyokawa, H., & Morimoto, M. (2021) · Developmental Dynamics · doi:10.1002/dvdy.345 · Cited by 11

Human Pluripotent Stem Cell-Derived Alveolar Organoids: Cellular Heterogeneity and Maturity

Jung, J., Yang, S., Kim, W. J., Rhee, C. K., & Hong, S. (2023) · Tuberculosis & respiratory diseases · doi:10.4046/trd.2023.0131 · Cited by 11

Abnormal liver differentiation and excessive angiogenesis in mice lacking Runx3

Lee, J., Lee, D., Bae, S., & Jung, H.-S. (2013) · Histochemistry and Cell Biology · doi:10.1007/s00418-013-1077-x · Cited by 11

Insights Into Human Development and Disease From Human Pluripotent Stem Cell Derived Intestinal Organoids

Daoud, A., & Múnera, J. O. (2019) · Frontiers in Medicine · doi:10.3389/fmed.2019.00297 · Cited by 11

Modeling Gastrointestinal Diseases Using Organoids to Understand Healing and Regenerative Processes

Ollivier, A., Mahé, M. M., & Guasch, G. (2021) · Cells · doi:10.3390/cells10061331 · Cited by 11

Genome Editing Human Pluripotent Stem Cells to Model β-Cell Disease and Unmask Novel Genetic Modifiers

George, M. N., Leavens, K. F., & Gadue, P. J. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.682625 · Cited by 11

Endodermal stem cell populations derived from pluripotent stem cells

Cheng, X., Tiyaboonchai, A., & Gadue, P. J. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2013.01.006 · Cited by 11

Getting Your Gut into Shape

Simons, B. D. (2013) · Science · doi:10.1126/science.1245288 · Cited by 11

Direct Lineage Reprogramming: Harnessing Cell Plasticity between Liver and PancreasPreprint

Ruzittu, S., Willnow, D., & Spagnoli, F. M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a035626 · Cited by 12

Hedgehog Signalling Pathway and Its Role in Shaping the Architecture of Intestinal Epithelium

Konopka, A., Gawin, K., & Barszcz, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212007 · Cited by 10

Distinct type I and II interferon responses direct cortical and medullary thymic epithelial cell development

Mohammed, A., Wang, W., Villanueva, M. A., Solomon, B. D., Slepicka, P. F., Hubka, K. M., Nguyen, H. D., Zheng, Z., Chavez, M., Yeh, C. Y., et al. (2025) · Science Immunology · doi:10.1126/sciimmunol.ado4720 · Cited by 11

MT1-MMP and its potential role in the vertebrate intestinal morphogenesis

Camargo, K. C., Gomes, J. R., Loddi, M. M., Sordi, R., Ayub, C. L. S. C., & Soares, M. A. D. M. (2016) · Acta Histochemica · doi:10.1016/j.acthis.2016.07.009 · Cited by 10

Id2 Determines Intestinal Identity through Repression of the Foregut Transcription Factor Irx5

Mori, K., Nakamura, H., Kurooka, H., Miyachi, H., Tamada, K., Sugai, M., Takumi, T., & Yokota, Y. (2018) · Molecular and Cellular Biology · doi:10.1128/mcb.00250-17 · Cited by 10

Polycomb Repressive Complexes: Shaping Pancreatic Beta-Cell Destiny in Development and Metabolic Disease

Varghese, S. S., & Dhawan, S. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.868592 · Cited by 11

Cellules souches embryonnaires humaines et iPS

Touboul, T., Vallier, L., & Weber, A. (2010) · médecine/sciences · doi:10.1051/medsci/201026121061 · Cited by 14

Proteomic Identification of RREB1, PDE6B, and CD209 Up-Regulated in Primitive Gut Tube Differentiated From Human Embryonic Stem Cells

Lee, D. H., Ko, J. J., Ji, Y. G., Chung, H., & Hwang, T. (2011) · Pancreas · doi:10.1097/mpa.0b013e3182223e35 · Cited by 10

Novel approaches for immune reconstitution and adaptive immune modeling with human pluripotent stem cells

Green, M. D., & Snoeck, H. (2011) · BMC Medicine · doi:10.1186/1741-7015-9-51 · Cited by 10

Metabolomic profiling of human pluripotent stem cell differentiation into lung progenitors

Leibel, S. L., Tseu, I., Zhou, A., Hodges, A. P., Yin, J., Bilodeau, C., Goltsis, O., & Post, M. (2022) · iScience · doi:10.1016/j.isci.2022.103797 · Cited by 10

Mouse embryonic dorsal root ganglia contain pluripotent stem cells that show features similar to ES cells and iPS cells

Ogawa, R., Fujita, K., & Ito, K. (2017) · Biology Open · doi:10.1242/bio.021758 · Cited by 10

Molecular Determinants of Lung Morphogenesis

Swarr, D. T., Wert, S. E., & Whitsett, J. A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-323-44887-1.00002-x · Cited by 10

An organoid and multi-organ developmental cell atlas reveals multilineage fate specification in the human intestinePreprint

Yu, Q., Kilik, U., Holloway, E. M., Tsai, Y.-H., Wu, A., Wu, J. H., Czerwinski, M. J., Childs, C. J., He, Z., Glass, I. A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.24.219147 · Cited by 12

An iPSC-based in vitro model recapitulates human thymic epithelial development and multi-lineage specification

Pretemer, Y., Gao, Y., Kanai, K., Yamamoto, T., Kometani, K., Ozaki, M., Nishigishi, K., Ikeda, T., Xu, H., Hotta, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62523-1 · Cited by 9

Study of the therapeutic effects of Painong powder on ulcerative colitis and the role of Platycodonis Radix in the prescription based on pharmacodynamic, pharmacokinetic, and tissue distribution analyses

Yu, H., Sun, H., Wang, K., Liang, X. H., Ding, Y., Chang, X., Guo, J. X., Peng, D., & Gui, S. Y. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114872 · Cited by 9

Cdx1b protects intestinal cell fate by repressing signaling networks for liver specification

Jin, Q., Gao, Y., Shuai, S., Chen, Y., Wang, K., Chen, J., Peng, J., & Gao, C. (2022) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2022.11.006 · Cited by 9

Flat mount preparation for whole-mount fluorescent imaging of zebrafish embryos

Frommelt, J., Liu, E. C., Bhaidani, A. B., Hu, B., Gao, Y., Ding, Y., & Lin, F. H. (2023) · Biology Open · doi:10.1242/bio.060048 · Cited by 9

Cell of Origin of Pancreatic cancer

Zheng, C., Wang, J., Wang, J., Zhang, Q., & Liang, T. (2024) · Pancreas · doi:10.1097/mpa.0000000000002301 · Cited by 12

RFX6 regulates human intestinal patterning and function upstream of PDX1

Sanchez, J. G., Rankin, S., Paul, E., McCauley, H. A., Kechele, D. O., Enriquez, J. R., Jones, N. Y., Greeley, S. A. W., Letourneau, L. R., Zorn, A. M., et al. (2024) · Development · doi:10.1242/dev.202529 · Cited by 9

Cell and tissue reprogramming: Unlocking a new era in medical drug discovery

Sen, C. K., Friday, A. J., & Roy, S. (2025) · Pharmacological Reviews · doi:10.1016/j.pharmr.2025.100077 · Cited by 9

Robust parameter design of human induced pluripotent stem cell differentiation protocols defines lineage-specific induction of anterior-posterior gut tube endodermal cells

Yasui, R., Sekine, K., Yamaguchi, K., Furukawa, Y., & Taniguchi, H. (2021) · Stem Cells · doi:10.1002/stem.3326 · Cited by 9

Hedgehog regulation of epithelial cell state and morphogenesis in the larynx

Ramachandran, J., Zhou, W., Bardenhagen, A. E., Nasr, T., Yates, E. R., Zorn, A. M., Ji, H., & Vokes, S. A. (2022) · eLife · doi:10.7554/elife.77055 · Cited by 9

Tmem88 confines ectodermal Wnt2bb signaling in pharyngeal arch artery progenitors for balancing cell cycle progression and cell fate decision

Zhang, M., Liu, J., Mao, A., Ning, G., Cao, Y., Zhang, W., & Wang, Q. (2023) · Nature Cardiovascular Research · doi:10.1038/s44161-023-00215-z · Cited by 9

Molecular and Physiological Determinants of Pulmonary Developmental Biology: a Review

Hameed, A., Sherkheli, M. A., Hussain, A., & Ul-haq, R. (2013) · American Journal of Biomedical Research · doi:10.12691/ajbr-1-1-3 · Cited by 9

The left-right asymmetry of liver lobation is generated by Pitx2c-mediated asymmetries in the hepatic diverticulum

Womble, M. A., Amin, N. M., & Nascone‐Yoder, N. M. (2018) · Developmental Biology · doi:10.1016/j.ydbio.2018.04.021 · Cited by 9

Engineering a second brain in a dish

Mahé, M. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.015 · Cited by 9

Vinblastine treatment decreases the undifferentiated cell contamination of human iPSC-derived intestinal epithelial-like cells

Ichikawa, M., Negoro, R., Kawai, K., Yamashita, T., Takayama, K., & Mizuguchi, H. (2021) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2021.01.005 · Cited by 9

Identification of downstream effectors of retinoic acid specifying the zebrafish pancreas by integrative genomics

López-Pérez, A. R., Balwierz, P. J., Lenhard, B., Müller, F., Wardle, F. C., Manfroid, I., Voz, M. L., & Peers, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-02039-y · Cited by 9

Differentiation of hiPS Cells into Definitive Endoderm for High-Throughput Screening

Bluhmki, T., Traub, S., Schruf, E., Garnett, J. P., Gantner, F., Bischoff, D., & Heilker, R. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9477-9_9 · Cited by 8

A dependency map enhanced with next-generation 3D cancer models

Neiswender, J. V., Maffa, S., Brenan, L., ElHarouni, D., Yun, Y., Boyle, I., Wienand, K., Inam, H., Bertea, T., Anderson, A., et al. (2026) · Nature · doi:10.1038/s41586-026-10843-7 · Cited by 9

Phosphorylated nuclear DICER1 promotes open chromatin state and lineage plasticity of AT2 tumor cells in lung adenocarcinomas

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Hhex and Prox1a synergistically dictate the hepatoblast to hepatocyte differentiation in zebrafish

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